Diastereomerism in palladium(II) allyl complexes of P,P-, P,S- and S,S-donor ligands, Ph2P(E)N(R)P(E′)Ph2 [R=CHMe2 or (S)-*CHMePh; E=E′=lone pair or S]: Solution behaviour, X-ray crystal structure and catalytic allylic alkylation reactions

Journal of Organometallic Chemistry

Volumn 676, Issue 1-2, 2003, Pages 22-37

  Mandal, S K Swadhin K ^a   Gowda, G A Nagana ^a   Krishnamurthy, Setharampattu S ^a   Zheng, Chong ^b   Li, Shoujian ^b   Hosmane, Narayan S ^b  

^a INDIAN INSTITUTE OF SCIENCE   (India)

^b NORTHERN ILLINOIS UNIVERSITY   (United States)

Author keywords

Allyl complexes; Allylic alkylation; P ligands; Palladium; S ligands; Stereodynamics by NMR spectroscopy

Indexed keywords

ALLYL COMPOUND; BENZENE DERIVATIVE; CATION; DIMER; LIGAND; PALLADIUM COMPLEX; PHOSPHORUS DERIVATIVE; SULFIDE;

ALKYLATION; ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL REACTION KINETICS; CHIRALITY; CRYSTAL STRUCTURE; DIASTEREOISOMER; ISOMERISM; NUCLEAR OVERHAUSER EFFECT; SOLID STATE; X RAY CRYSTALLOGRAPHY;

EID: 0038107196     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(03)00227-4     Document Type: Article

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